§ 360ee. Grants and contracts for development of drugs for rare diseases and conditions
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(a)Authority of Secretary The Secretary may make grants to and enter into contracts with public and private entities and individuals to assist in
(1)defraying the costs of developing drugs for rare diseases or conditions, including qualified testing expenses,
(2)defraying the costs of developing medical devices for rare diseases or conditions,
(3)defraying the costs of developing medical foods for rare diseases or conditions, and
(4)developing regulatory science pertaining to the chemistry, manufacturing, and controls of individualized medical products to treat individuals with rare diseases or conditions.
(b)Definitions For purposes of subsection (a):
(1)The term “qualified testing” means—
(A)human clinical testing—
(i)which is carried out under an exemption for a drug for a rare disease or condition under section 355(i) of this title (or regulations issued under such section); and
(ii)which occurs before the date on which an application with respect to such drug is submitted under section 355(b) of this title or under section 262 of title 42;
(B)preclinical testing involving a drug for a rare disease or condition which occurs after the date such drug is designated under section 360bb of this title and before the date on which an application with respect to such drug is submitted under section 355(b) of this title or under section 262 of title 42; and
(C)prospectively planned and designed observational studies and other analyses conducted to assist in the understanding of the natural history of a rare disease or condition and in the development of a therapy, including studies and analyses to—
(i)develop or validate a drug development tool related to a rare disease or condition; or
(ii)understand the full spectrum of the disease manifestations, including describing genotypic and phenotypic variability and identifying and defining distinct subpopulations affected by a rare disease or condition.
(2)The term “rare disease or condition” means
(1)in the case of a drug, any disease or condition which
(A)affects less than 200,000 persons in the United States, or
(B)affects more than 200,000 in the United States and for which there is no reasonable expectation that the cost of developing and making available in the United States a drug for such disease or condition will be recovered from sales in the United States of such drug,
(2)in the case of a medical device, any disease or condition that occurs so infrequently in the United States that there is no reasonable expectation that a medical device for such disease or condition will be developed without assistance under subsection (a), and
(3)in the case of a medical food, any disease or condition that occurs so infrequently in the United States that there is no reasonable expectation that a medical food for such disease or condition will be developed without assistance under subsection (a). Determinations under the preceding sentence with respect to any drug shall be made on the basis of the facts and circumstances as of the date the request for designation of the drug under section 360bb of this title is made.
(3)The term “medical food” means a food which is formulated to be consumed or administered enterally under the supervision of a physician and which is intended for the specific dietary management of a disease or condition for which distinctive nutritional requirements, based on recognized scientific principles, are established by medical evaluation.
(c)Authorization of appropriations For grants and contracts under subsection (a), there is authorized to be appropriated $6,904,110 for the period beginning on October 1, 2022 and ending on December 23, 2022.1
(Pub. L. 97–414, § 5, Jan. 4, 1983, 96 Stat. 2056; Pub. L. 98–551, § 4(b), Oct. 30, 1984, 98 Stat. 2817; Pub. L. 99–91, § 5, Aug. 15, 1985, 99 Stat. 391; Pub. L. 100–290, § 3(a)–(c), Apr. 18, 1988, 102 Stat. 90, 91; Pub. L. 105–115, title I, § 125(b)(2)(N), Nov. 21, 1997, 111 Stat. 2326; Pub. L. 107–281, § 3, Nov. 6, 2002, 116 Stat. 1993; Pub. L. 110–85, title XI, § 1112(b), Sept. 27, 2007, 121 Stat. 976; Pub. L. 112–144, title IX, § 906, July 9, 2012, 126 Stat. 1092; Pub. L. 114–255, div. A, title III, § 3015, Dec. 13, 2016, 130 Stat. 1094;
Pub. L. 115–52, title VI, § 603, Aug. 18, 2017, 131 Stat. 1048; Pub. L. 117–180, div. F, title V, § 5006, Sept. 30, 2022, 136 Stat. 2167; Pub. L. 117–229, div. C, title III, § 307, Dec. 16, 2022, 136 Stat. 2312; Pub. L. 117–328, div. FF, title III, § 3107, Dec. 29, 2022, 136 Stat. 5808.)
Connections101 cite this · traces to 14
Cited by 101 sections · top 60
U.S. Code
public-private-law
- Public Law 117-328Consolidated Appropriations Act, 2023
- Public Law 114-25521st Century Cures Act
- Public Law 115-52FDA Reauthorization Act of 2017
- Public Law 117-180Continuing Appropriations and Ukraine Supplemental Appropriations Act, 2023
- Public Law 117-229Further Continuing Appropriations and Extensions Act, 2023
- Public Law 117-79Accelerating Access to Critical Therapies for ALS Act
statute-compilations
- Sec. 307REAUTHORIZATION OF ORPHAN DRUG GRANTS
- Sec. 5FDA RARE NEURODEGENERATIVE DISEASE GRANT PROGRAM
- Sec. 3015AMENDMENTS TO THE ORPHAN DRUG GRANTS
- Sec. 906GRANTS AND CONTRACTS FOR THE DEVELOPMENT OF ORPHAN DRUGS
- Sec. 5grants and contracts for development of drugs for rare diseases and conditions
- Sec. 5006REAUTHORIZATION OF ORPHAN DRUG GRANTS
- Sec. 2GRANTS FOR RESEARCH ON THERAPIES FOR ALS
- Sec. 603REAUTHORIZATION OF ORPHAN GRANTS PROGRAM
statutes-at-large
- Public Law 112–144To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and medical devices, to establish user-fee programs for generic drugs and biosimilars, and for other purposes
- Public Law 97–414To amend the Federal Food, Drug, and Cosmetic Act to facilitate the development of drugs for rare diseases and conditions, and for other purposes
- Public Law 110–85To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and for medical devices, to enhance the postmarket authorities of the Food and Drug Administration with respect to the safety of drugs, and for other purposes
- Public Law 480
- Public Law 107–281To amend the Federal Food, Drug, and Cosmetic Act with respect to the development of products for rare diseases
- Public Law 98–551To revise and extend provisions of the Public Health Service Act relating to health promotion and disease prevention, to provide for the establishment of centers for research and demonstrations concerning health promotion and disease prevention, and for other purposes
- Public Law 117–79To direct the Secretary of Health and Human Services to support research on, and expanded access to, investigational drugs for amyotrophic lateral sclerosis, and for other purposes
- Public Law 117–229Making further continuing appropriations for the fiscal year ending September 30, 2023, and for other purposes
- Public Law 108–7
- Public Law 99–91To amend the orphan drug provisions of the Federal Food, Drug, and Cosmetic Act and related laws
- Public Law 480
- Public Law 114–255To accelerate the discovery, development, and delivery of 21st century cures, and for other purposes
- Public Law 106–387Making appropriations for Agriculture, Rural Development, Food and Drug Administration, and Related Agencies programs for the fiscal year ending September 30, 2001, and for other purposes
- Public Law 100–290To amend the Federal Food, Drug, and Cosmetic Act to revise the provisions respecting orphan drugs, and for other purposes
- Public Law 117–328Making consolidated appropriations for the fiscal year ending September 30, 2023, and for providing emergency assistance for the situation in Ukraine, and for other purposes
- Public Law 115–52To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs, medical devices, generic drugs, and biosimilar biological products, and for other purposes
- Public Law 117–180Making continuing appropriations for fiscal year 2023, and for other purposes
- Public Law 105–115To amend the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act to improve the regulation of food, drugs, devices, and biological products, and for other purposes
- Public Law 101–535To amend the Federal Food, Drug, and Cosmetic Act to prescribe nutrition labeling for foods, and for other purposes
register
- NoticesNotice of availability
- Rules and RegulationsFinal rule
- Proposed RulesAnnouncement of public meeting
- UnknownInterim rule
- NoticesNotice
- Rules and RegulationsProposed rule
- NoticesNotice of proposed rulemaking
- Presidential DocumentsProposed rule
- NoticesFinal rule
- NoticesNotice
- Rules and RegulationsFinal rule
- Proposed RulesFinal rule
- NoticesProposed rule
- NoticesProposed rule
- NoticesRequest for data and information
- NoticesNotice
Traces to 14 documents
U.S. Code
- New drugs§ 355
- Regulation of biological products§ 262
- Designation of drugs for rare diseases or conditions§ 360bb
- Recommendations for investigations of drugs for rare diseases or conditions§ 360aa
- Expanded access to unapproved therapies and diagnostics§ 360bbb
- Advisory councils§ 284a
- Definitions§ 632
- Short title§ 301
public-private-law
- 21st Century Cures ActPublic Law 114-255
- FDA Reauthorization Act of 2017Public Law 115-52
- Continuing Appropriations and Ukraine Supplemental Appropriations Act, 2023Public Law 117-180
- Further Continuing Appropriations and Extensions Act, 2023Public Law 117-229
- Consolidated Appropriations Act, 2023Public Law 117-328
- Accelerating Access to Critical Therapies for ALS ActPublic Law 117-79
40 references not yet in our index
- 1
- Pub. L. 97–414, § 5
- 96 Stat. 2056
- Pub. L. 98–551, § 4(b)
- 98 Stat. 2817
- Pub. L. 99–91, § 5
- 99 Stat. 391
- Pub. L. 100–290, § 3(a)
- 102 Stat. 90
- Pub. L. 105–115, title I, § 125(b)(2)(N)
- 111 Stat. 2326
- Pub. L. 107–281, § 3
- 116 Stat. 1993
- Pub. L. 110–85, title XI, § 1112(b)
- 121 Stat. 976
- Pub. L. 112–144, title IX, § 906
- 126 Stat. 1092
- 130 Stat. 1094
- 131 Stat. 1048
- 136 Stat. 2167
- 136 Stat. 2312
- 136 Stat. 5808
- Pub. L. 112–144, § 906(a)
- Pub. L. 112–144, § 906(b)
- Pub. L. 110–85
- Pub. L. 107–281
- Pub. L. 105–115
- Pub. L. 100–290, § 3(a)(1)
- Pub. L. 100–290, § 3(a)(2)
- Pub. L. 100–290, § 3(b)(3)
- Pub. L. 100–290, § 3(c)
- Pub. L. 99–91, § 5(a)(1)
- Pub. L. 99–91, § 5(a)(2)
- Pub. L. 99–91, § 5(b)
- Pub. L. 98–551
- Pub. L. 99–91
- section 8(a) of Pub. L. 99–91
- 135 Stat. 1533
- Pub. L. 107–281, § 2
- 116 Stat. 1992
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§ 360ee
Grants and contracts for development of drugs for rare diseases and conditions
Bills×33
Stat.×26
Fed. Reg.×16
Stat. Comp.×9
U.S.C.×8
Pub. L.×7
C.F.R.×2
Cite1
Pub. L.Pub. L. 97–414, § 5
Stat.96 Stat. 2056
Cites 54 · showing 12Cited by 101 across 7 sources